A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456457



Internal ID21114010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19707167..19840969hg38UCSC Ensembl
chr12:19860101..19993903hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38133803
hg19133803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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